Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT06277310

Wishes to Improve Support and Humanity at End-of-life in Safety-net Hospitals

Dignified and compassionate end-of-life (EOL) care is a cornerstone of high-quality, patient-centered care, but in safety-net hospitals EOL care is often overlooked, considered too late, or not at all. By eliciting and implementing final wishes for dying patients, the 3 Wishes Project (3WP) has demonstrated, in tertiary academic centers, that acts of compassion can improve the EOL experience and help families cope with loss. The investigators propose to implement the 3WP in safety-net hospitals where there are less resources and more diverse, disadvantaged patient populations, and hypothesize that there will be similar positive effects on the EOL experience for patients, families, and clinicians.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

LA General Hospital, Los Angeles, California, United States

Loading trial locations.

About this study

Compassionate end-of-life (EOL) care is foundational to medicine, but providing patients and families in safety-net hospitals (SNHs) with the sense that they are physically and emotionally supported during a patient's terminal hospitalization can be challenging. SNHs are public hospitals that primarily provide services to low-income and uninsured patients on a minimal budget. Although high quality EOL care is an important unmet need in SNHs, its provision is fraught with barriers and challenges. Language barriers, low health literacy, and cultural differences can make it difficult for families in SNHs to perceive empathy and support during the EOL. Deaths in the intensive care unit (ICU) for underserved families can be traumatic, and families of patients who die in the ICU often suffer from depression and post-traumatic stress disorder. Palliative care interventions are needed, but implementation is often resource-prohibitive.

The 3 Wishes Project (3WP) is a palliative care intervention that aims to achieve a dignified and compassionate EOL experience by empowering the clinical team to elicit and fulfill small wishes for critically ill patients who are dying in the ICU. Although the 3WP has been shown to improve a family's experience of their loved one's EOL care, ease bereavement, and enhance clinician work satisfaction in academic centers, it has not been implemented and evaluated in low-resource hospitals. The investigators believe that this patient-centered and clinician-partnered initiative can improve the EOL experience in SNHs, but that it must be adapted to the contextual differences and needs of low-resource hospitals.

Investigators propose to obtain and use stakeholder input to customize a multi-component 3WP Toolkit that will facilitate 3WP implementation in SNHs. Using the tailored Toolkit, the investigators will implement and evaluate the 3WP in the three SNHs of the Los Angeles County Department of Health Services. The investigators will conduct a pragmatic type 2 hybrid effectiveness-implementation study to evaluate the quality of EOL ICU care, bereaved families' psychological symptoms, and clinician burnout as compared to usual care. The Consolidated Framework for Implementation Research (CFIR) and the RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) framework will be used to guide a mixed-methods evaluation of the 3WP implementation in SNHs.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • For participation in the 3WP, if there was a decision to withdraw life support or the health care team agreed that the patient's probability of dying in the hospital or on discharge to hospice was >95% For surveys, next of kin/surrogate of a patient who died in the ICU during the study period For surveys, speaks English or Spanish

Exclusion criteria

  • <18 years old
  • does not speak english or spanish

Treatment and study plan

3 Wishes Project

Other

palliative care initiative in which clinicians elicits and implements small acts of kindness for dying patients and their families

Primary outcomes

  1. Families' assessment of the quality of end-of-life, particularly in emotional and spiritual support.

    Time frame: 3 months after patient's death (families will be surveyed 3 months after the date of death).

    Bereaved families of patients who died in the ICU will complete an after-death survey, which includes the Bereaved Family Survey (BFS). The BFS asks questions regarding the family's perception of the patient's end of life care. We will also use a question from the FS-ICU (family satisfaction with ICU) to assess whether family felt supported in final hours of patient's life.

Secondary outcomes

  1. Family anxiety and depression

    Time frame: 3 months after patient's death (families will be surveyed 3 months after the date of death).

    The Hospital Anxiety and Depression scale (HADS) will part of the after death survey.

  2. Nurse Burnout

    Time frame: 6 months and 1 year after

    Nurses will be asked to complete a survey (MBI) that evaluates nursing burnout before and after 3WP implementation.

  3. Family PTSD

    Time frame: 3 months after patient's death (families will be surveyed 3 months after the date of death).

    The PTSD Checklist for DSM-V (PCL-5) is part of the after death survey

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • LAC+USC Medical Center
  • National Institute of Nursing Research (NINR)
  • Olive View-UCLA Education & Research Institute

Registry information

Official study title

Personalized End of Life Care in Safety-Net Hospitals: Implementation of the 3 Wishes Project

Acronym: WISHES

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Feb 26, 2024
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.